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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712960Generated: October 30, 2026

Allylamine → Tert-butyl 2-(allylcarbamoyl)-4-(2,2-difluoroethyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/712960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantTriethylamineHCID 8471—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 86672461HCID 86672461—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductTert-butyl 2-(allylcarbamoyl)-4-(2,2-difluoroethyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 8667246083.2%

Reaction Steps

To 9-(tert-butoxycarbonyl)-4-(2,2-difluoroethyl)-1-oxa-4,9-diazaspiro[5.5]undecane-2-carboxylic acid (520 mg, 1.43 mmol), prop-2-en-1-amine (118 μL, 1.57 mmol) and T3P (2.12 mL of 50% w/w, 3.59 mmol) in 2-methyltetrahydrofuran (4 mL) was added triethylamine (597 μL, 4.28 mmol) at room temperature and the reaction mixture was stirred for 2 hours. The reaction mixture was then quenched with saturated NaHCO3 solution (3 mL) and stirred for an additional 10 minutes, then diluted with EtOAc and the layers were separated. The aqueous layer was extracted once more with EtOAc, and the combined organics were dried over Na2SO4, filtered and concentrated in vacuo to an oil. The residue was purified by silica gel column chromatography using 0-50% EtOAc in hexanes to yield tert-butyl 2-(allylcarbamoyl)-4-(2,2-difluoroethyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate (480 mg, 83%). ESI-MS m/z calc. 403.2. found 404.5 (M+1)+; Retention time: 1.78 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181273B2
Source datasetuspto-grants-2015_11
ORD IDord-92c49f00bde3471d9c4cfe48194d831c
Source noteuspto-grants-2015_11